A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3579787



Internal ID18878068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:89896137..90077315hg38UCSC Ensembl
Innerchr2:89934947..90116157hg19UCSC Ensembl
Innerchr2:89571989..89753462hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38181179
hg19181211
hg18181474
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1007834
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3579787
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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